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用于延长循环寿命锂氧电池的、由薄金属铱层保护的独立式碳纳米纤维。

Free-Standing Carbon Nanofibers Protected by a Thin Metallic Iridium Layer for Extended Life-Cycle Li-Oxygen Batteries.

作者信息

Nam Jong Seok, Jung Ji-Won, Youn Doo-Young, Cho Su-Ho, Cheong Jun Young, Kim Min Soo, Song Seok-Won, Kim Sang-Joon, Kim Il-Doo

机构信息

Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea.

出版信息

ACS Appl Mater Interfaces. 2020 Dec 16;12(50):55756-55765. doi: 10.1021/acsami.0c13325. Epub 2020 Nov 25.

Abstract

It is evident that the exhaustive use of fossil fuels for decades has significantly contributed to global warming and environmental pollution. To mitigate the harm on the environment, lithium-oxygen batteries (LOBs) with a high theoretical energy density (3458 Wh kgLiO) compared to that of Li-ion batteries (LIBs) have been considered as an attractive alternative to fossil fuels. For this purpose, porous carbon materials have been utilized as promising air cathodes owing to their low cost, lightness, easy fabrication process, and high performance. However, the challenge thus far lies in the uncontrollable formation of LiCO at the interface between carbon and LiO, which is detrimental to the stable electrochemical performance of carbon-based cathodes in LOBs. In this work, we successfully protected the surface of the free-standing carbon nanofibers (CNFs) by coating it with a layer of iridium metal through direct sputtering (CNFs@Ir), which significantly improved the lifespan of LOBs. Moreover, the Ir would play a secondary role as an electrochemical catalyst. This all-in-one cathode was evaluated for the formation and decomposition of LiO during (dis)charging processes. Compared with bare CNFs, the CNFs@Ir cathode showed two times longer lifespan with 0.2 V lower overpotentials for the oxygen evolution reaction. We quantitatively calculated the contents of CO in LiCO formed on the different surfaces of the bare CNFs (63% reduced) and the protected CNFs@Ir (78% reduced) cathodes after charging. The protective effects and the reaction mechanism were elucidated by ex situ analyses, including scanning electron microscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy.

摘要

显而易见,数十年来对化石燃料的过度使用极大地导致了全球变暖和环境污染。为减轻对环境的危害,与锂离子电池(LIBs)相比具有高理论能量密度(3458 Wh kgLiO)的锂氧电池(LOBs)被视为化石燃料的一种有吸引力的替代品。为此,多孔碳材料因其低成本、轻质、易于制造工艺和高性能而被用作有前景的空气阴极。然而,迄今为止的挑战在于在碳与LiO的界面处不可控地形成LiCO,这对LOBs中碳基阴极的稳定电化学性能不利。在这项工作中,我们通过直接溅射在独立的碳纳米纤维(CNFs)表面成功涂覆了一层铱金属(CNFs@Ir),从而显著提高了LOBs的寿命。此外,Ir还将作为电化学催化剂发挥辅助作用。对这种一体化阴极在(充)放电过程中LiO的形成和分解进行了评估。与裸CNFs相比,CNFs@Ir阴极的寿命延长了两倍,析氧反应的过电位降低了0.2 V。我们定量计算了充电后在裸CNFs(减少63%)和受保护的CNFs@Ir(减少78%)阴极不同表面上形成的LiCO中CO的含量。通过包括扫描电子显微镜、透射电子显微镜和X射线光电子能谱在内的非原位分析阐明了保护效果和反应机理。

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